Ethyl Acetate

Aroma chemical · Fruity

ethereal, fruity, pineapple, brandy — top note.

Aroma illustration for Ethyl Acetate: a clear droplet with ripples and a pineapple, for its ethereal and pineapple notes. It illustrates smell associations, not the material or its source.Skeletal formula of Ethyl Acetate (Ethyl ethanoate), C4H8O2, drawn from PubChem's 2D record. Stereochemistry is not shown.
Aroma View: an illustration of what Ethyl Acetate smells like (ethereal, pineapple), drawn by RUŌOD Lab — not its appearance or its source.Skeletal formula drawn by RUŌOD Lab from PubChem's 2D record (CID 8857). Stereochemistry is not shown; the coloured background is decoration.
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By the RUŌOD Lab TeamRevision 1Updated

In short

Ethyl acetate is the simplest common fruity ester, found in fruit and fermented drinks. It has a light, ethereal, fruity odour and evaporates very quickly.

What Ethyl Acetate smells like

JECFA describes ethyl acetate as a colourless liquid, volatile at low temperatures, with a fragrant, acetic, ethereal odour. The Hazardous Substances Data Bank records an ether-like odour reminiscent of pineapple, and fruity with a brandy note. Fraterworks describes a sweet, ethereal, fruity aroma of pineapple, grape and pear drops, a highly volatile top note with ethereal liquor nuances of brandy and rum.

Leading note
Ethereal
Supporting facets
Pineapple, brandy
Faint facets
Acetic
Character
Volatile, light
  • ethereal
  • fruity
  • pineapple
  • brandy

What makes Ethyl Acetate distinctive

A thin, ethereal fruitiness that is gone in moments — the lightest of the fruity esters.

Concentration and dilution

Fraterworks also sells it as a 10% solution in DPG, and warns against inhaling it.

How Ethyl Acetate is used

Fraterworks uses it to give lift and brightness to top notes and to round off the rough edges of sharp top notes, and notes its use as an inexpensive solvent.

Typical role: lift (adds diffusion and radiance, especially at the top).

How Ethyl Acetate differs from similar materials

Propionaldehyde
Propionaldehyde is sharp and pungent; ethyl acetate is the softer, ethereal-fruity top note, and both are gone in moments.

Each difference compares the published descriptions of the two materials. Smell varies with grade, supplier and dilution; compare them side by side on blotters before substituting one for another.

Formulation considerations

Extremely volatile and highly flammable; it disappears from a blotter almost at once.

Identity and classification

Type
Aroma chemical
Origin
Occurs in nature
Odour family
Fruity
Note position
Top note
Physical form at room temperature
Liquid
Also known as
Ethyl ethanoate, Acetic ether
CAS number
141-78-6
Molecular formula
C4H8O2
Molecular weight
88.11 g/mol
IUPAC name
ethyl acetate

The CAS number, formula and molecular weight are taken from PubChem compound 8857, whose own record lists this CAS number; checked 24 October 2026.

Safety and compliance

Hazard classification of the neat substance, as PubChem summarises it, read 26 October 2026. It has a harmonised EU classification (Regulation (EC) No 1272/2008, Annex VI): H225 highly Flammable liquid and vapor; H319 causes serious eye irritation; H336 may cause drowsiness or dizziness. Companies notifying the ECHA C&L Inventory classify it (5,233 reports): H336 may cause drowsiness or dizziness (99.7% of reports); H319 causes serious eye irritation (91.1% of reports). 3 of the reports find it does not meet the hazard criteria. Unless it is harmonised, this is the notifiers' own classification, not a binding one.

This page is general information, not a safety assessment or a specification. Confirm identity, composition, IFRA status and allergen content from your supplier's documents for the lot you hold.

Materials it works with

Ethyl Acetate is also suggested as a partner on the pages for Propionaldehyde.

Used in formulas and accords

Used in 6 published formulas

Ethyl Acetate is an ingredient in 5 accords and 1 base in the Formula & Accord Library.

Further reading

Questions about Ethyl Acetate

Is Ethyl Acetate natural or synthetic?

The molecule occurs in nature. Commercial Ethyl Acetate may be made by synthesis or obtained from natural sources, so check the supplier's specification if the distinction matters to you.

What is the CAS number of Ethyl Acetate?

141-78-6. It was checked against PubChem on 24 October 2026.

Which published formulas use Ethyl Acetate?

Ethyl Acetate is used in 6 published formulas in the RUŌOD Lab Formula & Accord Library, including Açaí Accord, Blackberry Accord and Champagne Accord. Each is listed with a link under "Used in formulas and accords" on this page.

Sources

Your own records, next to the reference

Keep your own record of Ethyl Acetate — supplier, cost, stock, dilutions and where it is used — in RUŌOD Lab's material library.